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首页> 外文期刊>Acta oncologica. >Prostate-specific antigen after salvage radiotherapy for postprostatectomy biochemical recurrence predicts long-term outcome including overall survival
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Prostate-specific antigen after salvage radiotherapy for postprostatectomy biochemical recurrence predicts long-term outcome including overall survival

机译:挽救后的前列腺特异性抗原在后浆化生化复发中预测包括整体存活的长期结果

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摘要

Background: For patients with recurrent prostate cancer after radical prostatectomy (RP), salvage radiotherapy (SRT) is a second chance of cure. However, depending on risk factors, 40-70% of the patients experience further progression. With a focus on the pre- and post-SRT serum level of the prostate-specific antigen (PSA), we assessed the determinants of the long-term outcome after SRT.Patient and methods: Between 1997 and 2011, 464 patients received 3D-conformal SRT with median 66.6Gy. The median PSA level before SRT was 0.31ng/ml. In our retrospective analysis, post-SRT progression was defined as either a rising PSA 0.2ng/ml above the nadir, or the application of anti-androgens or clinical recurrence. A PSA 0.1ng/ml was termed undetectable. We analyzed the data with the Kaplan-Meier method (Logrank test) and multivariable Cox regression.Results: The median follow-up was 5.9 years. Overall, 178 patients had recurrence, 13 developed distant metastases and 30 died. Univariate, a pre-RP PSA 10ng/ml, pathological stage pT 3, Gleason score 8, positive surgical margins, a pre-SRT PSA 0.2ng/ml and a post-SRT PSA nadir 0.1ng/ml correlated with fewer and later second recurrences. In a multivariable Cox model, pT, Gleason score, margin status and pre-SRT PSA were significant covariates of progression. If the post-SRT PSA response was included in the regression analysis, then a nadir 0.1ng/ml was the strongest risk factor. Initiating SRT at a PSA 0.2ng/ml correlated with a post-SRT PSA 0.1ng/ml. Men who achieved an undetectable post-SRT PSA nadir also had lower rates of metastases and a better overall survival. However, there were too few events for Cox regression analysis of these two endpoints.Conclusions: Early SRT at a PSA 0.2ng/ml correlates with re-achieving an undetectable PSA, which predicts improved freedom from progression and metastases and better overall survival.
机译:背景:对于患有自由基前列腺切除术(RP)后的经常性前列腺癌的患者,救赎放疗(SRT)是治疗的第二次。但是,根据危险因素,40-70%的患者体验进一步进展。重点关注前列腺特异性抗原(PSA)的SRT后血清水平,我们评估了SRT.Patient和方法后的长期结果的决定因素:1997年至2011年间,464名患者接受3D-共形SRT与中位数66.6Gy。 SRT之前的中位PSA水平为0.31ng / ml。在我们的回顾性分析中,后SRT进展定义为Nadir上方0.2ng / ml,或抗血糖或临床复发的应用。 PSA <0.1ng / ml被称为未检测到的。我们用Kaplan-Meier方法(Logrank测试)和多变量Cox回归分析了数据。结果:中位随访5.9岁。总体而言,178名患者具有复发,13名突出的远离转移和30名死亡。单变量,rp预rp psa& 10ng / ml,病理阶段pt <3,gleason ade <8,正外科缘,前Srt PSA <0.2ng / ml和后SRT PSA Nadir& 0.1ng / ml与较少和后期的第二次复发相关。在多变量的Cox模型中,PT,Gleason评分,边距和Pre-SRT PSA是重要的进展变协调性。如果在回归分析中包含后SRT PSA响应,那么Nadir 0.1ng / ml是最强的风险因素。在PSA& 0.2ng / ml与后SRT PSA& 0.1ng / ml相关联的SRT。达到未检测到的后SRT PSA Nadir的男性也具有较低的转移率和更好的整体生存。然而,对这两个终点的Cox回归分析的事件太少了。结论:PSA的早期SRT <0.2ng / ml与重新实现不可检测的PSA相关,这预测来自进展和转移的改善和更好的整体生存。

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  • 来源
    《Acta oncologica.》 |2018年第3期|共6页
  • 作者单位

    Univ Hosp Ulm Dept Radiat Oncol Albert Einstein Allee 23 D-89081 Ulm Germany;

    Univ Hosp Ulm Dept Radiat Oncol Albert Einstein Allee 23 D-89081 Ulm Germany;

    Esslingen Hosp Dept Radiat Oncol Esslingen Germany;

    Charite Dept Radiat Oncol Berlin Germany;

    Charite Dept Radiat Oncol Berlin Germany;

    Charite Dept Radiat Oncol Berlin Germany;

    Univ Hosp Ulm Dept Radiat Oncol Albert Einstein Allee 23 D-89081 Ulm Germany;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
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